This work reports the synthesis of
pyridyltriazol-functionalized
UiO-66 (UiO stands for University of Oslo), namely, UiO-66-Pyta, from
UiO-66-NH2 through three postsynthetic modification (PSM)
steps. The good performance of the material derives from the observation
that partial formylation (∼21% of −NHCHO groups) of
H2BDC-NH2 by DMF, as persistent impurity, takes
place during the synthesis of the UiO-66-NH2. Thus, to
enhance material performance, first, the as-synthesized UiO-66-NH2 was deformylated to give pure UiO-66-NH2. Subsequently,
the pure UiO-66-NH2 was converted to UiO-66-N3 with a nearly complete conversion (∼95%). Finally, the azide–alkyne[3+2]-cycloaddition
reaction of 2-ethynylpyridine with the UiO-66-N3 gave the
UiO-66-Pyta. The porous MOF was then applied for the solid-phase extraction
of palladium ions from an aqueous medium. Affecting parameters on
extraction efficiency of Pd(II) ions were also investigated and optimized.
Interestingly, UiO-66-Pyta exhibited selective and superior adsorption
capacity for Pd(II) with a maximum sorption capacity of 294.1 mg g–1 at acidic pH (4.5). The limit of detection (LOD)
was found to be 1.9 μg L–1. The estimated
intra- and interday precisions are 3.6 and 1.7%, respectively. Moreover,
the adsorbent was regenerated and reused for five cycles without any
significant change in the capacity and repeatability. The adsorption
mechanism was described based on various techniques such as FT-IR,
PXRD, SEM/EDS, ICP-AES, and XPS analyses as well as density functional
theory (DFT) calculations. Notably, as a case study, the obtained
UiO-66-Pyta after palladium adsorption, UiO-66-Pyta-Pd, was used as
an efficient catalyst for the Suzuki–Miyaura cross-coupling
reaction.